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HRID 1427039作成日:2026年10月26日

Dimethyl Sulfoxide → N-(4-((6-(2-Ethoxyethoxy)-1H-indol-5-yl)oxy)pyridin-2-yl)acetamide

https://huagongshe.com/reaction/1427039

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物N-(4-Chloropyridin-2-yl)acetamideHCID 22832129—
反応物Potassium tert-butoxideHCID 23665647—
反応物6-(2-Ethoxyethoxy)-1H-indol-5-olHCID 86730341—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-((6-(2-Ethoxyethoxy)-1H-indol-5-yl)oxy)pyridin-2-yl)acetamideHCID 8673034248%

反応条件

温度150 °C

反応手順

Dimethylsulfoxide (20 mL) was added to a mixture of 6-(2-ethoxyethoxy)-1H-indol-5-ol described in Production Example 24-5 (3.28 g, 14.8 mmol), N-(4-chloropyridin-2-yl)acetamide described in Production Example 1-5 (2.78 g, 16.3 mmol), and potassium tert-butoxide (1.83 g, 16.3 mmol) under nitrogen atmosphere at room temperature. The liquid mixture was stirred at 150° C. overnight. The reaction liquid was allowed to stand to cool to room temperature and then diluted with water and ethyl acetate. The organic layer was washed with a saturated saline solution and dried over anhydrous sodium sulfate, and then the drying agent was separated by filtration. The filtrate was concentrated under vacuum. The residue was purified with silica gel column chromatography (n-heptane:ethyl acetate=1:1-0:1-ethyl acetate:methanol=99:1-19:1) to obtain the title compound (2.5 g, 48%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08933099B2
出典データセットuspto-grants-2015_01
ORD IDord-9cd462329aa84014b77b2e0e837efd04
出典メモuspto-grants-2015_01